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临床试验/JPRN-UMIN000048352
JPRN-UMIN000048352已完成未知

Survey on prescription of the new laxatives in patients with chronic constipation under daily clinical practice, using real-world data - Survey on prescription of the new laxatives in the patients with chronic constipation

EA Pharma Co., Ltd. Medical Science group Medical department0 个研究点目标入组 19,295 人开始时间: 2022年7月12日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
发起方
入组人数
19,295

研究概览

简要总结

ELO discontinuation (DC) rate within 360 days was 78.7%. Inpatients, end-stage renal failure, and diagnosis of constipation by obstetrics/gynecology or oncology departments were identified as risks for DC. Diagnosis of constipation, diabetes mellitus, Parkinson's disease, or use of laxative (LX) was lower risk of DC. The prescription rate of stimulants and saline LX decreased and nearly half of them discontinued these LX within 360 days. Results of M4000E were published in JPT 52(3) 253-67 in Japanese.

研究设计

研究类型
Observational

入排标准

年龄范围
ot applicable 至 ot applicable(—)
性别
All

入选标准

  • 未提供

排除标准

  • The patients who have no hospital visits from 180 days to 1 day before the index date.

研究者

发起方
EA Pharma Co., Ltd. Medical Science group Medical department

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